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Query: UMLS:C1275122 (TEM)
 21,810 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

To resolve discrepancies between its enzymological activity and its in vitro or in vivo activity, 6-acetylmethylenepenicillanic acid (Ro 15-1903), a potent beta-lactamase inhibitor, was investigated for its chemical stability and its ability to penetrate the bacterial cell envelope. Although Ro 15-1903 was fairly stable in water or saline, it was found to be unstable in a rich medium, in mouse plasma and in human serum. Decomposition half-lives in Tryptic Soy Broth (TSB) and mouse plasma were determined by spectrometry to be 1.3 hours and 12 minutes respectively. These values were confirmed by a biochemical method for determination of Ro 15-1903. Furthermore, a large enhancement of the in vitro activity was noticed when the assay medium was changed from TSB to a synthetic medium in which Ro 15-1903 was more stable. The ampicillin-potentiating activity marginally increased if a permeability mutant harboring the R6K plasmid, which codes for TEM-1 beta-lactamase production, was used instead of the wild-type strain. These results prove that the chemical instability of Ro 15-1903 is the main cause of its disproportionally low activity in vitro and in vivo. Ro 15-1903 is not nonspecifically inactivated by proteins, since it did not lose its activity after incubation with bovine serum albumin (50 mg/ml) for 2 hours at 37 degrees C. It seems to react specifically with beta-lactamase.
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PMID:Studies on 6-acetylmethylenepenicillanic acid (Ro 15-1903). III. Relationship between in vitro activity and chemical stability. 631 68

The preparation and high resolution observation of frozen hydrated thin sections has been studied by transmission electron microscopy (TEM and STEM) on model systems, including pure water, protein solutions, catalase crystals, myelin sheath and various tissues. The state of the ice is determined by electron diffraction. Mass measurement in the electron microscope is used to determine section thickness and control hydration. An adequate depth of vitrified material for sectioning can be obtained from many biological suspensions or untreated tissues. Frozen hydrated sections around 100 nm thick can be produced under optimal conditions from vitreous ice or from vitrified biological samples. Sectioning, transfer and observation in the electron microscope is feasible without alteration of the sample hydration or its initial vitrification. Biological structures can be preserved and observed down to 10 nm. Under favourable working conditions, specimen compression during sectioning and electron beam damage are the factors limiting high resolution observations.
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PMID:Electron microscopy of frozen hydrated sections of vitreous ice and vitrified biological samples. 635 May 98

The fine-structural analysis of injuries and injury-related damages of the arteries in the head and neck region, such as vital endothelial injuries resulting from death by hanging, is of considerable importance in legal medicine, as it involves numerous forensic problems. The problems and difficulties of vessel preparation, including the occurrence of artefacts, have been widely discussed in medical journals, indicating the necessity for a special method of preparation to be developed. This method has to take individual differences of the autopsy material into consideration, including osmolarity changes caused by hypoxia, and autolysis. The method developed by us and described here meets these conditions. Optimization and standardization of the method was achieved by perfusion fixation of the vascular system in situ. The particular characteristics of the vessels involved made it necessary to open the skull. After removing the upper half of the brain and applying a partially permeable sealing to the skull base, we proceeded with the perfusion, using slightly hyperosmotic perfusion media (450-680 mOsm) via a hydrostatic system, and keeping pressure and flow rates low (max. 65 cm H2O). The perfusion technique we developed, and which is described in detail, has proven suitable for the preparation of other vessels as well, which is demonstrated on the venae cerebri superiores. The method of preparation was designed to provide conditions for a routine application of SEM, LM and TEM for forensic purposes.
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PMID:A preparative technique for morphological analysis of the vessels in head and neck for medico-legal examinations. 636 17

A method for preparing and handling large, clean, distortion-free cut surfaces through small and delicate tissues for correlated SEM/TEM examination is described. In this method, tissues are fixed according to conventional protocols; however, instead of critical-point-drying after fixation, tissues are first embedded in polyethylene glycol (PEG), a water-soluble waxy solid. Tissue blocks are easily oriented and sectioned to the desired regions, immersed in a solvent to remove PEG, critical-point-dried, and examined with an SEM. The same tissue blocks can be reworked for TEM by immersing in propylene oxide and embedding in an epoxy resin.
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PMID:A method for exposing the internal anatomy of small and delicate tissues for correlated SEM/TEM studies using polyethylene glycol embedding. 636 35

Microanalytical experiments have been performed to answer the question whether the main cellular cation, K+, follows the water distribution in the striated muscle cell or whether K+ follows the distribution of negative fixed charges (beta- and gamma-carboxyl groups of aspartic and glutamic acid residues). Subcellular localization of K and/or of the K surrogates Rb, Cs, and Tl has been investigated by the following methods: Chemical precipitation of K with tetraphenylborate. Autoradiography of alkali-metals and Tl in air-dried and frozen-hydrated preparations. TEM visualization of electron dense Cs and Tl in sections of freeze-dried and plastic embedded muscle. X-ray microanalysis of air-dried myofibrils and muscle cryosections. The experiments consistently show that K, Rb, Cs, and Tl do not follow the water distribution but are mainly accumulated in the A band, especially in the marginal regions, and at Z lines. The same sites preferentially accumulate Cs or uranyl cations when sections of freeze-dried, embedded muscle are exposed to these electron microscopic stains. It is concluded that the detected uneven distribution of K, Rb, Cs, and Tl in muscle is neither a freeze-drying artifact nor an embedding artifact and may result from a weak ion binding to the beta- and gamma-carboxyl groups of cellular proteins.
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PMID:Subcellular distribution of potassium in striated muscles. 648 3

The structure of the acini in the swine sweat gland is described here at the TEM level. The acini of the sweat gland in the pig is formed by 2 secretory cell types: dark seromucous cells and clear cells. The dark seromucous cells are actively secretory and their secretion is apocrine. The clear cells seem to be involved in an active transport of water and electrolytes through their cytoplasms.
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PMID:The fine structure of the swine sweat gland. I. The acini. 672 Dec 13

Freeze-substitution is a technique suitable for the preparation of unicellular and multi-cellular plant and animal specimens for conventional light microscopy, TEM and SEM. It is also widely used as a means of preparing animal and plant tissues for the localization of water soluble substances by analytical electron microscopy, autoradiography or visual detection of precipitates. The technical requirements of preparation, together with an evaluation of the procedures, are presented for various applications. Careful selection and evaluation of freezing technique, substitution solvent and regime are required for meaningful results.
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PMID:Freeze-substitution. 675 Jan 31

The inorganic phase in dentin with dentinogenesis imperfecta was investigated, using the correlated techniques of high resolution TEM, X-ray diffraction analyses, infrared absorption spectroscopy, thermogravimetry, and chemical and electron microprobe analyses. It was shown that crystallites in dentin with dentinogenesis imperfecta are of normal size (from 3 to 6 lattice planes thick), but less numerous than in normal dentin. Electron microprobe analyses indicated significant differences in the mineral content of dentin with dentinogenesis imperfecta compared to normal dentin. A higher Ca/P ratio, a loss in Ca and P, and a severe significant loss in Mg, corroborated by chemical analyses, were recorded. The main component of the inorganic phase in dentin with dentinogenesis imperfecta was found to be poorly crystallized carbonated apatite. It is suggested that the water content, greatly increased in dentin with dentinogenesis imperfecta, is at least partly related to lattice water tightly bound to the inorganic phase.
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PMID:The inorganic phase in dentinogenesis imperfecta. 694 58

Little is known about the physiological effects of short-term fasting in avian species. The present study was developed to examine the alimentary mucosal changes in fasted birds by scanning and transmission electron microscopy. Chickens of various ages were fasted for periods of 3, 5, and 7 days. Water was provided ad libitum. At the end of the fasting periods the birds were sacrificed along with ad libitum fed controls. Tissue samples from crop, duodenum, and ileum were processed by standard methods for scanning and transmission electron microscopy (SEM and TEM). The SEM samples were prepared by vacuum drying methods. The TEM samples were embedded in Spurrs embedding medium. Mucosal sloughing was observed in the crop and small intestine with SEM only in fasted birds. With TEM, separation was observed between the mucosal cells of fasted birds with membranous whorls in these spaces. Sloughed cells may be an endogenous protein source for the fasting bird.
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PMID:Influence of short term fasting on chicken alimentary canal mucosa. 726 57

Columnals of Neocrinus blakei, a modern species of stalked crinoid, were studied using a variety of analytical techniques. Analyses of the magnesium calcite of the crinoid stereom using powder X-ray diffraction and electron microprobe analysis yield a composition of Ca 88Mg 12C03. Scanning transmission electron microscopy (STEM) microanalytical data indicate that Mg incorporation into the calcite structure of the crinoid stereom is random and homogeneous to at least the 20 nm level. There appear to be no variations in composition at this level either within or between structural entities of the crinoid columnal stereom. TEM reveals a heterogeneity of contrast which may be due to incorporation of organic material or some other substance which is non-crystalline in character. Single-crystal X-ray diffraction data indicate that the individual skeletal plates are single crystals which yield diffuse and imperfect X-ray reflections due to a mosaic structure. Subsequent selected area electron diffraction (SAD) photographs via TEM, using various sizes of SAD apertures, indicate that the crystallites making up the mosaic structure are (order of magnitude) about 1.0 micrometer in size. The presence of mosaic structure in the single crystal skeletal elements may at least in part explain the lack of cleavage in fracture surfaces of echinoderm skeletal material. Based on these data, as well as data from skeletal elements of other deep water, stalked crinoids, we feel that these results may be applicable to crinoids in general, at least those existing in relatively constant temperature environments. The single-crystal nature of crinoid high magnesium calcite, and its remarkable homogeneity of composition suggest that a large "vital effect" (i. e., biologic control of skeletal deposition) mediates the mineralization process.
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PMID:Biomineralization on crinoid echinoderms. Characterization of crinoid skeletal elements using TEM and STEM microanalysis. 733 May 80


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